{"schemaVersion":"jobsearcher.job.v1","id":"32effa09203e5850800d2e36","url":"https://jobsearcher.com/jobs/32effa09203e5850800d2e36","canonicalUrl":"https://jobsearcher.com/jobs/32effa09203e5850800d2e36","title":"Process Engineer","description":"Responsibilities:\n\nLead projects in manufacturing process areas to achieve process efficiencies such as increase in process yield, quality improvements, cycle time/throughput, and cost reduction initiatives.\n\nGather and analyze process data using statistical process control methodology. Develop action plan to increase process robustness, prevent product loss, and control quality impact. Participate in process performance monitoring such as Track & Trend.\n\nResponsible for providing technical support in the resolution of shop floor situations and executing assigned tasks as required by the operational area.\n\nLead investigations by following a structure problem solving approach and employing sound, scientific principles when identifying root cause and developing recommendations related to product and process. Generate technical justification to support and/or document process deviations/investigations and determine impact in product quality, yield, and product registration.\n\nPart of cross-functional team responsible for implementation of site projects/initiatives (continuous improvement, cost reduction, capacity increase, etc.) that lead to process remediation.\n\nProject management of smaller team, short duration projects within larger projects. Responsibility may include project coordination, monitoring, reporting, meeting management, and team communication.\n\nLead the implementation of process validation for operational changes, new raw materials, and introduction of new process/technology. Generate technical justification determining impact of change and protocols/reports/manufacturing documents that support its execution. Assist the execution of experimental, demonstration, and validation lots.\n\nMaintain up-to-date product process documentation and assure they are in compliance with applicable procedures and regulations. Writes justification memos and scientific reports of quality controls and manufacturing documents.\n\nProvide scientific and technical support during regulatory audits and agency inspections.\n\nDemonstrate accountability and responsibility for EHS performance and compliance through active participation and support of Client's EHS program.\n\nRequirements:\n\nBS or MS or PhD in Chemistry or Engineering (Chemical, Mechanical, Bio-chemical, or other relevant scientific field).\n\n5–7 years of technical experience in Process/Manufacturing/Project Engineering or similar role.\n\nTechnical knowledge in fundamentals of pharmaceutical process (sterile product manufacturing).\n\nEffective verbal and written communication skills in both English.\n\nTop 3–5 Required Skills / Experience:\n\nTechnical transfer.\n\nSterile drug product manufacturing.\n\nGMP pharma process validation.\n\nExperience working with CMOs.\n\nAbility to travel (domestic and/or international).\n\nKey Stakeholders:\n\nManufacturing.\n\nQuality.\n\nSupply Chain.\n\nOperational Excellence.\n\nEngineering.\n\nEHS.\n\n#J-18808-Ljbffr","company":"Creative Solutions Services","rawCompany":"creative solutions services","city":"Antioch","state":"IL","isRemote":false,"isActive":false,"createdAt":"2026-06-20T04:44:29.953Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325998","title":"All Other Miscellaneous Chemical Product and Preparation Manufacturing","slug":"all-other-miscellaneous-chemical-product-and-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer","description":"Responsibilities:\n\nLead projects in manufacturing process areas to achieve process efficiencies such as increase in process yield, quality improvements, cycle time/throughput, and cost reduction initiatives.\n\nGather and analyze process data using statistical process control methodology. Develop action plan to increase process robustness, prevent product loss, and control quality impact. Participate in process performance monitoring such as Track & Trend.\n\nResponsible for providing technical support in the resolution of shop floor situations and executing assigned tasks as required by the operational area.\n\nLead investigations by following a structure problem solving approach and employing sound, scientific principles when identifying root cause and developing recommendations related to product and process. Generate technical justification to support and/or document process deviations/investigations and determine impact in product quality, yield, and product registration.\n\nPart of cross-functional team responsible for implementation of site projects/initiatives (continuous improvement, cost reduction, capacity increase, etc.) that lead to process remediation.\n\nProject management of smaller team, short duration projects within larger projects. Responsibility may include project coordination, monitoring, reporting, meeting management, and team communication.\n\nLead the implementation of process validation for operational changes, new raw materials, and introduction of new process/technology. Generate technical justification determining impact of change and protocols/reports/manufacturing documents that support its execution. Assist the execution of experimental, demonstration, and validation lots.\n\nMaintain up-to-date product process documentation and assure they are in compliance with applicable procedures and regulations. Writes justification memos and scientific reports of quality controls and manufacturing documents.\n\nProvide scientific and technical support during regulatory audits and agency inspections.\n\nDemonstrate accountability and responsibility for EHS performance and compliance through active participation and support of Client's EHS program.\n\nRequirements:\n\nBS or MS or PhD in Chemistry or Engineering (Chemical, Mechanical, Bio-chemical, or other relevant scientific field).\n\n5–7 years of technical experience in Process/Manufacturing/Project Engineering or similar role.\n\nTechnical knowledge in fundamentals of pharmaceutical process (sterile product manufacturing).\n\nEffective verbal and written communication skills in both English.\n\nTop 3–5 Required Skills / Experience:\n\nTechnical transfer.\n\nSterile drug product manufacturing.\n\nGMP pharma process validation.\n\nExperience working with CMOs.\n\nAbility to travel (domestic and/or international).\n\nKey Stakeholders:\n\nManufacturing.\n\nQuality.\n\nSupply Chain.\n\nOperational Excellence.\n\nEngineering.\n\nEHS.\n\n#J-18808-Ljbffr","datePosted":"2026-06-20T04:44:29.953Z","dateModified":"2026-06-20T04:44:29.953Z","hiringOrganization":{"@type":"Organization","name":"Creative Solutions Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Antioch","addressRegion":"IL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"32effa09203e5850800d2e36"},"url":"https://jobsearcher.com/jobs/32effa09203e5850800d2e36"}}